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Nicolet is50 infrared spectrometer

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Nicolet iS50 is an infrared spectrometer designed for analytical applications. It is capable of recording infrared spectra of various samples. The core function of the Nicolet iS50 is to analyze the interaction between infrared radiation and the sample material, providing information about the chemical composition and molecular structure of the analyzed substance.

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10 protocols using nicolet is50 infrared spectrometer

1

FT-IR Spectroscopic Analysis of Samples

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For obtaining the FT-IR spectra, the samples were prepared by mixing the sample and KBr tableting at a ratio of 1:200 in a dry environment. Then, the FT-IR spectra were obtained at the wavenumber range of 4000–500 cm−1 with a Nicolet Is50 infrared spectrometer (Thermo Fisher Scientific, Wal than, MA, USA).
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2

Infrared Spectroscopy of Beta-Cyclodextrin

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The appropriate amount of β-CD, the physical mixture, and a-β-CD were analyzed by a Nicolet IS50 infrared spectrometer (Thermo Fisher Scientific, Waltham, MA, USA). The wavenumber range was 400–4000 cm−1 [38 (link)].
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3

Physicochemical Characterization of Chitosan Adsorbents

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The scanning electron microscopy (SEM, Merlin Compact, Germany Carl Zeiss) method was used to describe the morphologies of CSA, CSP, and CSEN. X-ray diffraction (XRD, D8 ADVANCE, Germany Bruker) analyses of CSH, CSA, CSP, and CSEN were performed to analyze the crystalline structures. The scanning rate was set at 2°/min with an operating voltage of 40 kV and a current of 40 mA. The chemical compositions of the four chitosan adsorbents were analyzed using the attenuated total reflection unit on the Thermo Scientific Nicolet iS50 infrared spectrometer (USA, ATR-FTIR). The specific surface areas of CSH, CSA, CSP, and CSEN were estimated using the Brunauer–Emmett–Teller (BET) analysis (Quantachrome, Autosorb-IQ, USA). The absorbance was measured using a visible-light spectrophotometer (UNICO, 2100, Shanghai, China). Before SEM, BET, and ATR-FTIR testing, CSH was subjected to elution with anhydrous ethanol and then dried using supercritical CO2 drying to avoid the disturbance of residual water, while the other three chitosan adsorbents were tested directly.
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4

Characterization of CS-based Coatings

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The morphology of the deposited CS-based coatings was examined by SEM using a JEOL JSM–7500F Field Emission Scanning Electron Microscope equipped with an EDX detector.
FT-IR spectra were measured by a Thermo Scientific Nicolet is50 Infrared Spectrometer. Spectra were recorded in a mid-infrared range (500–4000 cm−1) using an attenuated total reflection (ATR) accessory with a diamond crystal.
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5

Spectroelectrochemical Study of Gold Thin Films

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The
spectra were recorded using Nicolet iS50 infrared spectrometer (Thermo
Fisher Scientific Inc.) equipped with liquid nitrogen cooled MCT-A
detector and custom-made single-reflection accessory. The incident
angle was set at 60°, and the spectral resolution was 4 cm–1. The spectra are displayed in absorbance units defined
as A = log(I0/I), where I0 and I correspond to the intensities of IR radiation observed for the reference
and the sample, respectively. In all experiments, we have used all-glass
spectroelectrochemical cell with platinum foil as a counter electrode
and Ag/AgCl/sat. KCl as a reference electrode. The working electrode
was a thin gold film deposited on a reflectance plane of a silicon
hemispherical prism accordingly to the procedure described in the
literature.26 (link) PGSTAT101 potentiostat (Metrohm
Autolab) was utilized to control electrode potential. Omnic 9 software
(Thermo Fisher Scientific Inc.) was used for data processing.
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6

Starch Short-Range Orders Analysis

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The FTIR spectra of the samples were obtained on a Nicolet iS50 infrared spectrometer (Thermo Fisher, Waltham, MA, USA) equipped with an ATR accessory from 4000 to 400 cm−1. Each spectrum was recorded at a resolution of 4 cm−1 for 32 scans against the air as the background. The spectra in the range of 1200 to 800 cm−1 were smoothed, baseline corrected, and deconvoluted using the Omnic 8.2 software. The ratio of the peak intensity at 995 cm−1 to that at 1022 cm−1 (R995/1022) was used to indicate the relative amount of starch short-range orders.
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7

Infrared Spectroscopy of Lipid Bilayers

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All spectra were collected using a Nicolet iS50 infrared spectrometer (Thermo Fisher Scientific Inc.) equipped with a liquid-nitrogen-cooled MCT-A detector and custom-made single-reflection accessory. The incident angle was set at 55°, and the spectral resolution was 4 cm−1. The spectra are presented in absorbance units A = log(I0/I), where I0 and I correspond to the single-beam intensities of IR radiation observed for the reference and the sample, respectively. In all experiments, we used a silicon hemispherical prism. The bilayer was deposited on the planar surface of the prism by spreading of lipid vesicles. The refractive indices used for the molecular orientation calculations were 3.42 for Si, 1.45 for lipid bilayer, and 1.32 for D2O. Data processing was performed with Omnic 9 software (Thermo Fisher Scientific Inc., Waltham, MA, USA).
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8

Multimodal Characterization of Carbon Dots

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The fluorescence spectra were recorded by a Cary Eclipse fluorescence spectrophotometer (Agilent Technologies, USA). UV-Vis absorption spectra were measured in a UV-2450 spectrophotometer (Shimadzu Corporation, Japan). Transmission electron microscopy (TEM) images were obtained from FEI Talos F200S (Thermo Fisher Scientific, USA). The fluorescence lifetime decay curves of CDs were recorded by a FS5 fluorescence spectrometer (Edinburgh Instruments, Britain). Fourier transform infrared spectroscopy (FTIR) was obtained from a NICOLET iS50 Infrared Spectrometer (Thermo Fisher Scientific, USA).
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9

Characterization of Modified Rubber Powder

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The conversion and grafting ratio of the HRP were calculated [42 (link),43 (link)]. The weight of the WRP was W1, the weight of added AM was W2, and the weight of the product was W3. The equation of the yield and grafting ratio is expressed as: Conversion=W3W1W2
Graftingratio=W3W1W1
FT-IR spectra of the functional groups on the surface of the rubber powder were recorded on a Nicolet-is50 infrared spectrometer (Thermo Fisher, New York, NY, USA) in the range of 4000–400 cm−1 with a 2 cm−1 resolution using a KBr pellet.
The impact of the different AM and BPO qualities on the hydrophilicity of the modified rubber powder was measured using the water contact angle. After the samples were pressed into a tablet, the contact angles of the samples were tested using a DSA25 Contact Angle Meter instrument (Kruss, Berlin, Germany). Each sample was tested three times, and the average value was taken as the result.
Thermogravimetric analyses of the modified rubber powder were tested using a TGA2 Thermal Gravimetric Analyzer (Mettler Toledo, Bern, Switzerland). The sample was heated from 35 °C to 800 °C at the rate of 10 °C/min under a nitrogen atmosphere.
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10

Characterization of Probiotic Microcapsules

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The morphology of the wet microcapsules was analyzed using an optical microscope (Nikon ECLIPSE Ti-S, Japan). The morphology of the dried microcapsules was evaluated using a Phenom ProX Desktop Scanning Electron Microscope (Phenom Scientific, Netherlands).
2.9 FT-IR spectra and XRD pattern analysis FT-IR spectra of the whey protein, pectin, probiotic-loaded microcapsules and the control were recorded on a Nicolet iS50 infrared spectrometer (Thermo Fisher, USA) using a KBr pellet method scanning in the range of 400-4000 cm -1 [26] (link). XRD pattern of the probiotic-loaded microcapsules and the control were performed using an X-ray diffractometer (Rigaku Ultima 4, Japan), following a published method [27] (link), the test conditions were as follows: Cu radiation of wavelength 1.5406 Å, pipeline pressure 40 kV, angle range 3-80 ° (2θ), scanning speed 0.5°/min.
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